Evidence map›Paper›PMID 35056760›Full record

ReviewMolecules (Basel, Switzerland)2022

PCSK9 as a Target for Development of a New Generation of Hypolipidemic Drugs.

Nikolay Kuzmich, Elena Andresyuk, Yuri Porozov, Vadim Tarasov, Mikhail Samsonov, Nina Preferanskaya, Valery Veselov, Renad Alyautdin

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
7.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  3. International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Nikolay KuzmichLaboratory of Drug Safety, Smorodintsev Research Institute of Influenza, WHO National Influenza Centre of Russia, 15/17 Professor Popov Street, 197376 Saint-Petersburg, Russia.
Elena AndresyukWorld-Class Research Center "Digital Biodesign and Personalized Healthcare", I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.
Yuri PorozovWorld-Class Research Center "Digital Biodesign and Personalized Healthcare", I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.
Vadim TarasovDepartment of Pharmacology, I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.
Mikhail SamsonovDepartment of Pharmacology, I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.ORCID 0000-0003-2685-1623
Nina PreferanskayaDepartment of Pharmacology, I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.
Valery VeselovDepartment of Pharmacology, I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.
Renad AlyautdinDepartment of Pharmacology, I.M. Sechenov First Moscow State Medical University, 8/2 Trubetskaya Street, 119991 Moscow, Russia.
Sechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PCSK9 has now become an important target to create new classes of lipid-lowering drugs. The prevention of its interaction with LDL receptors allows an increase in the number of these receptors on the surface of the cell membrane of hepatocytes, which leads to an increase in the uptake of cholesterol-rich atherogenic LDL from the bloodstream. The PCSK9 antagonists described in this review belong to different classes of compounds, may have a low molecular weight or belong to macromolecular structures, and also demonstrate different mechanisms of action. The mechanisms of action include preventing the effective binding of PCSK9 to LDLR, stimulating the degradation of PCSK9, and even blocking its transcription or transport to the plasma membrane/cell surface. Although several types of antihyperlipidemic drugs have been introduced on the market and are actively used in clinical practice, they are not without disadvantages, such as well-known side effects (statins) or high costs (monoclonal antibodies). Thus, there is still a need for effective cholesterol-lowering drugs with minimal side effects, preferably orally bioavailable. Low-molecular-weight PCSK9 inhibitors could be a worthy alternative for this purpose.

Indexed as

Proprotein Convertase 9HepatocytesHumansHypolipidemic AgentsMolecular Targeted TherapyReceptors, LDLHypolipidemic AgentsPCSK9 protein, humanProprotein Convertase 9Receptors, LDLantihyperlipidemic therapyLDLRlipid-lowering drugsPCSK9PCSK9 inhibitors

Identifiers

PMID35056760
PMCPMC8778893
OpenAlexW4205447903

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.